Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
  • A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
  • A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
  • A61K8/4966—Triazines or their condensed derivatives

Definitions

• the present invention relates to cosmetic and dermatological light protection formulations, in particular skin-care cosmetic and dermatological light protection formulations.
• UVC range rays having a wavelength of less than 290 nm
• UVB range rays in the range between 290 nm and 320 nm, the so-called UVB range, cause erythema, simple sunburn or even burns of greater or lesser severity.
• the narrower range around 308 nm is stated as the erythema activity maximum of sunlight.
• UVA range For the range between about 320 nm and about 400 nm, the so-called UVA range, it is also important to have available filter substances, since the rays thereof can also cause damage. Thus, it has been proved that UVA radiation leads to damage to the elastic and collagenic fibres of connective tissue, which makes the skin age prematurely, and that it is to be regarded as a cause of numerous phototoxic and photoallergic reactions.
• the damaging effect of UVB radiation can be intensified by UVA radiation.
• UV radiation can also lead to photochemical reactions, the photochemical reaction products then intervening in the skin metabolism.
• Such photochemical reaction products are chiefly free-radical compounds, for example hydroxyl radicals.
• Undefined free-radical photoproducts which are formed in the skin itself can also show uncontrolled secondary reactions because of their high reactivity.
• singlet oxygen a non-radical excited state of the oxygen molecule, may also occur under UV irradiation, as can short-lived epoxides and many others.
• Singlet oxygen for example, is distinguished from the triplet oxygen normally present (free-radical ground state) by an increased reactivity. Nevertheless, excited, reactive (free-radical) triplet states of the oxygen molecule also exist.
• UV radiation is furthermore counted among ionizing radiation. There is therefore the risk of ionic species also being formed during UV exposure, which then in turn are capable of intervening oxidatively in biochemical processes.
• UVB filter is 4,4',4"-(1,3,5-triazine-2,4,6-triyltriimino)-trisbenzoic acid tris(2-ethylhexyl ester), synonym: 2,4,6-tris-[anilino-(p-carbo-2'-ethyl-1'-hexyloxy)]-1,3,5-triazine. ##STR1##
• This UVB filter substance is marketed by BASF Aktiengesellschaft under the trade name UVINUL® T 150, and is distinguished by good UV absorption properties.
• UVB filter The main disadvantage of this UVB filter is the poor solubility in lipids.
• Known solvents for this UVB filter can dissolve a maximum of about 15% by weight of this filter, corresponding to about 1-1.5% by weight of dissolved, and therefore active, UV filter substance.
• the invention also particularly relates to the use of one or more emulsifiers chosen from the group of substances of the general structural formula ##STR3## wherein R 1 , R 2 and R 3 independently of one another are chosen from the group which comprises: H and branched and unbranched, saturated and unsaturated fatty acid radicals having 8 to 24 carbon atoms, in which up to three aliphatic hydrogen atoms can be replaced by hydroxyl groups, and n is a number from 2 to 8, as a solvent, solubilizing agent or solubilizer for 4,4',4"-(1,3,5-triazine-2,4,6-triyltriimino)-trisbenzoic acid tris(2-ethylhexyl ester), in particular for use in light protection compositions.
• R 1 , R 2 and R 3 independently of one another are chosen from the group which comprises: H and branched and unbranched, saturated and unsaturated fatty acid radicals having 8 to 24 carbon atoms, in which up to three
• a prerequisite for the usability of the active compound combinations according to the invention for the purposes according to the invention is of course cosmetic or dermatological acceptability of the substances on which they are based.
• emulsifiers used according to the invention chosen from the group of substances of the general structural formula ##STR4## wherein R 1 , R 2 and R 3 independently of one another are chosen from the group which comprises: H and branched and unbranched, saturated and unsaturated fatty acid radicals having 8 to 24 carbon atoms, in which up to three aliphatic hydrogen atoms can be replaced by hydroxyl groups, and n is a number from 2 to 8, a stabilization of solutions of 4,4',4"-(1,3,5-triazine-2,4,6-triyltriimino)-trisbenzoic acid tris(2-ethylhexyl ester) is effected, since the latter substance not only has a poor solubility but also readily crystallizes out again from its solution.
• the invention therefore also relates to a process for stabilizing solutions of 4,4',4"-(1,3,5-triazine-2,4,6-triyltriimino)-trisbenzoic acid tris(2-ethylhexyl ester), characterized in that an active content of emulsifiers used according to the invention is added to such solutions.
• JP-Hei-04/178316 indeed describes cosmetic formulations having a content of emulsifiers which fall under the structural formula given under (b), but no indication of the present invention is given therein.
• the total amount of 4,4',4"-(1,3,5-triazine-2,4,6-triyltriimino)-trisbenzoic acid tris(2-ethylhexyl ester) in the finished cosmetic or dermatological formulations is advantageously chosen from the range of 0.1-10.0% by weight, preferably 0.5-6.0% by weight, based on the total weight of the formulations.
• the total amount of one or more emulsifiers used according to the invention chosen from the group of substances of the general structural formula ##STR5## wherein R 1 , R 2 and R 3 independently of one another are chosen from the group which comprises: H and branched and unbranched, saturated and unsaturated fatty acid radicals having 8 to 24 carbon atoms, in which up to three aliphatic hydrogen atoms can be replaced by hydroxyl groups, and n is a number from 2 to 8, in the finished cosmetic or dermatological formulations is advantageously chosen from the range of 0.01-250.0% by weight, preferably 0.1-10.0% by weight, more preferably 0.5-6.0% by weight, based on the total weight of the formulations.
• weight ratios of 4,4',4"-(1,3,5-triazine-2,4,6-triyltriimino)-trisbenzoic acid tris(2-ethylhexyl ester) and one or more emulsifiers used according to the invention chosen from the group of substances of the general structural formula ##STR6## wherein R 1 , R 2 and R 3 independently of one another are chosen from the group which comprises: H and branched and unbranched, saturated and unsaturated fatty acid radicals having 8 to 24 carbon atoms, in which up to three aliphatic hydrogen atoms can be replaced by hydroxyl groups, and n is a number from 2 to 8, from the range from 1:10 to 10:1, preferably 1:4 to 4:1.
• Cosmetic and dermatological formulations according to the invention moreover comprise inorganic pigments based on metal oxides and/or other metal compounds which are sparingly soluble or insoluble in water, in particular the oxides of titanium (TiO 2 ), zinc (ZnO), iron (for example Fe 2 O 3 ), zirconium (ZrO 2 ), silicon (SiO 2 ), manganese (for example MnO), aluminium (Al 2 O 3 ) or cerium (for example Ce 2 O 3 ), mixed oxides of the corresponding metals and mixtures of such oxides.
• the pigments are particularly preferably those based on TiO 2 .
• the inorganic pigments are present in hydrophobic form, i.e. they are given a water-repellent treatment on the surface.
• This surface treatment can comprise providing the pigments with a thin hydrophobic layer by processes known per se.
• Such a process comprises, for example, producing the hydrophobic surface layer by a reaction in accordance with
• n and m in this equation are stoichiometric parameters to be inserted as required, and R and R' are the desired organic radicals.
• Pigments hydrophobicized, for example, analogously to German Offenlegungsschrift 33 14 742 are of advantage.
• Advantageous TiO 2 pigments are obtainable, for example, under the trade name MT 100 T from TAYCA.
• the total amount or inorganic pigments, in particular hydrophobic inorganic micropigments, in the finished cosmetic or dermatological formulations is advantageously chosen from the range of 0.1-30% by weight, preferably 0.1-10.0, preferably 0.5-6.0% by weight, based on the total weight of the formulations.
• the cosmetic and/or dermatological light protection formulations according to the invention can have the customary compositions and be used for cosmetic and/or dermatological protection from light, and furthermore for treatment, care and cleansing of the skin and/or hair and as a make-up product in decorative cosmetics.
• the cosmetic and dermatological formulations according to the invention are applied to the skin and/or hair in an adequate amount in the manner customary for cosmetics.
• sunscreen compositions which are in the form of a sunscreen composition are particularly preferred. These can advantageously additionally comprise at least one further UVA filter and/or at least one further UVB filter and/or at least one inorganic pigment, preferably an inorganic micropigment.
• the cosmetic and dermatological formulations according to the invention can comprise cosmetic auxiliaries such as are usually used in such formulations, for example preservatives, bactericides, perfumes, substances for preventing foaming, dyestuffs, pigments which have a colouring action, thickeners, moisturizing and/or humectant substances, fats, oils, waxes or other customary constituents of a cosmetic or dermatological formulation, such as alcohols, polyols, polymers, foam stabilizers, electrolytes, organic solvents or silicone derivatives.
• cosmetic auxiliaries such as are usually used in such formulations, for example preservatives, bactericides, perfumes, substances for preventing foaming, dyestuffs, pigments which have a colouring action, thickeners, moisturizing and/or humectant substances, fats, oils, waxes or other customary constituents of a cosmetic or dermatological formulation, such as alcohols, polyols, polymers, foam stabilizers, electrolytes, organic solvents
• antioxidants An additional content of antioxidants is in general preferred. All the antioxidants suitable or customary for cosmetic and/or dermatological uses can be used according to the invention as favourable antioxidants.
• the antioxidants are advantageously chosen from the group consisting of amino acids (for example glycine, histidine, tyrosine and tryptophan) and derivatives thereof, imidazoles (for example urocaninic acid) and derivatives thereof, peptides, such as D,L-carnosine, D-carnosine, L-carnosine and derivatives thereof (for example anserine), carotinoids, carotenes (for example ⁇ -carotene, ⁇ -carotene and lycopene) and derivatives thereof, chlorogenic acid and derivatives thereof, liponic acid and derivatives thereof (for example di-hydroliponic acid), aurothioglucose, propylthiouracil and other thiols (for example thioredoxin, glutathione, cysteine, cystine, cystamine and the glycosyl, N-acetyl, methyl, ethyl, propyl, amyl, butyl and lauryl, palmito
• the amount of the abovementioned antioxidants (one or more compounds) in the formulations is preferably 0.001 to 30% by weight, particularly preferably 0.05-20% by weight, in particular 1-10% by weight, based on the total weight of the formulation.
• vitamin E and/or derivatives thereof are the antioxidant or antioxidants, it is advantageous to choose the particular concentrations thereof from the range of 0.001-10% by weight, based on the total weight of the formulation.
• vitamin A or vitamin A derivatives or carotenes or derivatives thereof are the antioxidant or antioxidants, it is advantageous to choose the particular concentrations thereof from the range of 0.001-10% by weight, based on the total weight of the formulation.
• oils such as triglycerides of capric or caprylic acid, but preferably castor oil;
• esters of fatty acids with alcohols of low C number for example with isopropanol, propylene glycol or glycerol, or esters of fatty alcohols with alkanoic acids of low C number of with fatty acids;
• silicone oils such as dimethylpolysiloxanes, diethylpolysiloxanes, diphenylpolysiloxanes and mixed forms thereof.
• the aqueous phase of the formulations according to the invention advantageously comprises
• alcohols, diols or polyols of low C number, and ethers thereof preferably ethanol, isopropanol, propylene glycol, glycerol, ethylene glycol, ethylene glycol monoethyl or monobutyl ether, propylene glycol monomethyl, monoethyl or monobutyl ether, diethylene glycol monomethyl or monoethyl ether and analogous products, and furthermore alcohols of low C number, for example ethanol, isopropanol, 1,2-propanediol, glycerol and, in particular, one or more thickeners, which can advantageously be chosen from the group consisting of silicon dioxide, aluminium silicates, polysaccharides and derivatives thereof, for example hyaluronic acid, xanthan gum and hydroxypropylmethylcellulose, particularly advantageously from the group consisting of polyacrylates, preferably a polyacrylate from the group consisting of the so-called carbopols, for example carbopols of
• the cosmetic or dermatological light protection formulations advantageously comprise inorganic pigments, in particular micropigments, for example in amounts of 0.1% by weight to 30% by weight, preferably in amounts of 0.5% by weight to 10% by weight, but in particular 1% by weight to 6% by weight, based on the total weight of the formulations.
• the light protection formulations according to the invention can advantageously comprise further substances which absorb UV radiation in the UVB range, the total amount of filter substances being, for example, 0.1% by weight to 30% by weight, preferably 0.5 to 10% by weight, in particular 1 to 6% by weight, based on the total weight of the formulations, in order to provide cosmetic formulations which protect the skin from the entire range of ultraviolet radiation. They can also be used as sunscreen compositions.
• the further UVB filters can be oil-soluble or water-soluble.
• Advantageous oil-soluble UVB filter substances are, for example:
• 3-benzylidenecamphor derivatives preferably 3-(4-methylbenzylidene) camphor, 3-benzylidenecamphor;
• 4-aminobenzoic acid derivatives preferably 2-ethylhexyl 4-(dimethylamino)benzoate and amyl 4-(dimethylamino benzoate;
• ester of cinnamic acid preferably 2-ethylhexyl 4-methoxycinnamate and isopentyl 4-methoxycinnamate;
• benzophenone preferably 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-methoxy-4'-methylbenzophenone, 2,2'-dihydroxy-4-methoxybenzophenone;
• esters of benzalmalonic acid preferably di(2-ethylhexyl) 4-methoxybenzalmalonate.
• Advantageous water-soluble UVB filter substances are, for example:
• salts of 2-phenylbenzimidazole-5-sulphonic acid such as its sodium, potassium or its triethanolammonium salt, and the sulphonic acid itself;
• sulphonic acid derivatives of benzophenones preferably 2-hydroxy-4-methoxybenzophenone-5-sulphonic acid and salts thereof;
• sulphonic acid derivatives of 3-benzylidenecamphors such as, for example, 4-(2-oxo-3-bornylidenemethyl)benzenesulphonic acid, 2-methyl-5-(2-oxo-3-bornylidenemethyl)benzenesulphonic acid and salts thereof.
• UVB filters mentioned which can be used in combination with the active compound combinations according to the invention is, of course, not intended to be limiting.
• UVA filters which have usually been contained to date in cosmetic formulations.
• These substances are preferably derivatives of dibenzoylmethane, in particular 1-(4'-tert-butylphenyl)-3-(4'-methoxyphenyl)-propane-1,3-dione and 1-phenyl-3-(4'-isopropylphenyl)propane-1,3-dione.
• the invention also relates to these combinations and to formulations which comprise these combinations. The amounts used for the UVB combination can be employed.
• the invention also relates to a process for the preparation of the cosmetic and/or dermatological light protection formulations according to the invention, which is characterized in that, in a manner known per se, the 4,4',4"-(1,3,5-triazine-2,4,6-triyltriimino)-triabenzoic acid tris(2-ethylhexyl ester) is suspended in one or more alkanecarboxylic acids or an oily phase having a content of alkanecarboxylic acids, while stirring uniformly and if appropriate while heating, and, if desired, the mixture is homogenized, the mixture is combined with further lipid components, if appropriate, and with one or more emulsifiers, if appropriate, thereafter the oily phase is mixed with the aqueous phase, into which a thickener has been incorporated, if appropriate, and which preferably has about the same temperature as the oily phase, and the mixture is homogenized, if desired, and allowed to cool to room temperature. After cooling to room temperature,

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• 1996
  • 1996-01-25 DE DE19602618A patent/DE19602618A1/de not_active Ceased
• 1997
  • 1997-01-16 ES ES97100567T patent/ES2220998T3/es not_active Expired - Lifetime
  • 1997-01-16 AT AT97100567T patent/ATE268157T1/de not_active IP Right Cessation
  • 1997-01-16 DE DE59711676T patent/DE59711676D1/de not_active Expired - Lifetime
  • 1997-01-16 EP EP97100567A patent/EP0786246B1/de not_active Expired - Lifetime
  • 1997-01-22 JP JP9021897A patent/JPH09202723A/ja active Pending
  • 1997-01-24 US US08/788,147 patent/US5968483A/en not_active Expired - Fee Related

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